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Data / Product recalls / Threshold Enterprises Ltd

Threshold Enterprises Ltd: 5 recalls from 2017 to 2019 (FDA)

Threshold Enterprises Ltd, Scotts Valley, CA, is named in 5 recalls from 2017 to 2019: all from the FDA. The latest, on October 30, 2019, covers Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets, 60 tablets Manufactured for.... Hazard: Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation. Source: FDA F-0061-2020.

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Country
United States
Location
Scotts Valley, CA
Agencies
U.S. Food and Drug Administration
First recall
May 10, 2017
Latest recall
October 30, 2019

Recalls

Each recall is listed once, with the role this firm has in it. Roles: recalling firm (5).

DateAgencyProductHazardUnitsRemedySold atRoleSource
October 30, 2019FDASource Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets, 60 tablets Manufactured for: Source Natural, Inc. PO Box 2118...Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation.1,822 bottlesVoluntary recall, Class III, terminatedRecalling firmaccessdata.fda.gov
March 6, 2019FDAPlanetary Herbals Mullein Lung Complex; 1000 mg; 15 count, item number PF0003; 90 count - Item number PF0002; 180 count, Item number PF0106 and 90 +...Recall of Mullein Lung Complex due to a labeling error which indicates the incorrect excipient profile (inactive ingredients).16, 542 unitsVoluntary recall, Class II, terminatedRecalling firmaccessdata.fda.gov
August 9, 2017FDAPlanetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 60 count - UPC 0 21078 10214 4...Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.36 bottles - 7 x 120 count and 29 x 60 count.Voluntary recall, Class II, terminatedRecalling firmaccessdata.fda.gov
July 19, 2017FDASource Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium... and 1 more productDietary supplements contain low levels of undeclared boron55,354 units (first of 2 products)Voluntary recall, Class II, terminatedRecalling firmaccessdata.fda.gov
May 10, 2017FDASource Naturals Dietary Supplement Vitamin D-3; Bioactive Form for Bone and Immune Health 2000 IU per serving, 500% DV. Other ingredients: Vegetable...Testing of Vitamin D-3 as a result of a consumer complaint found specific lots to have lower concentrations than product specifications of ingredient labeling.129,331 total unitsVoluntary recall, Class II, terminatedRecalling firmaccessdata.fda.gov

By agency

AgencyRecallsLatest
U.S. Food and Drug Administration5October 30, 2019

Categories

Where each agency publishes its recalls

Updated October 30, 2019. Read from U.S. Food and Drug Administration recall data. CC0 1.0 (openFDA). Recalls are as the agencies published them: the CPSC, FDA (food enforcement reports) and NHTSA. A firm is one firm only when its exact name and country match; the CPSC and FDA print no firm ID. Stores are listed only when the agency's sold-at text names them, and an agency often adds that more stores sold the product. Categories are grouped by SpecStream from the words in the agency's title and product text. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.